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Blood|May 13, 2011
Exome sequencing reveals germline NPAT mutation as a candidate risk factor for Hodgkin lymphomaSilva Saarinen, Mervi Aavikko, Kristiina Aittomäki, et al.European Urology|June 25, 2018
Large-scale Analysis Demonstrates Familial Testicular Cancer to have Polygenic AetiologyChey Loveday, Philip Law, Kevin Litchfield, et al.Nature Genetics|April 4, 2008
Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1Christopher I Amos, Xifeng Wu, Peter Broderick, et al.The Journal of Clinical Endocrinology and Metabolism|July 30, 2013
Genome-wide association study on differentiated thyroid cancerAleksandra Köhler, Bowang Chen, Federica Gemignani, et al.Plos Genetics|September 24, 2010
Allelic variation at the 8q23.3 colorectal cancer risk locus functions as a cis-acting regulator of EIF3HAlan M Pittman, Silvia Naranjo, Sanni E Jalava, et al.Human Molecular Genetics|August 2, 2013
Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancerNicola Whiffin, Sara E Dobbins, Fay J Hosking, et al.Plos One|April 1, 2015
Common variation at 1q24.1 (ALDH9A1) is a potential risk factor for renal cancerMarc Y R Henrion, Mark P Purdue, Ghislaine Scelo, et al.Cancer Discovery|May 16, 2012
Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinomaJianxin Shi, Nilanjan Chatterjee, Melissa Rotunno, et al.Human Molecular Genetics|May 3, 2011
Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genesLuis G Carvajal-Carmona, Jean-Baptiste Cazier, Angela M Jones, et al.Nature Communications|October 2, 2015
Genome-wide association study identifies multiple susceptibility loci for gliomaBen Kinnersley, Marianne Labussière, Amy Holroyd, et al.Pageof 11